224 Results for "

cyclohexanone

" in MedChemExpress (MCE) Product Catalog:
Products (224)

224 Results for "cyclohexanone" in MCE Product Catalog:

Cat. No.: HY-N11955
CAS No.: 91741-17-2
Cyclo(Ile-Leu) is a Alkaloids product that can be isolated from From Penicillium oxalicum .
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Cat. No.: HY-P1935
CAS No.: 36357-32-1
Cyclo(Ala-Pro) is an anticancer agent that is toxic to cancer cells such as A549, HCT-116 and HepG2 .
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Cat. No.: HY-P2092
CAS No.: 15136-34-2
Synonyms: Cyclo(Leu-Trp)
Cyclo(L-leucyl-L-tryptophyl) (Cyclo(-Leu-Trp)) is a cyclic dipeptide that inhibits a various of bacteria and fungi. Cyclo(L-leucyl-L-tryptophyl) is a melatonin receptor agonist and is also used as a bitter ligand .
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Cat. No.: HY-W549438
CAS No.: 2862-51-3
Research Areas:  

Others

Cyclo(Phe-Phe) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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Cat. No.: HY-P10222
Research Areas:  

Cancer

Cyclo CRLLIF is a dual inhibitor for hypoxia inducible factor (HIF) 1 and 2, which disrupts the interaction of both HIF1-α and HIF2-α with HIF1-β, with affinity for HIF1-α and HIF2-α PAS-B domains KD of 14.5 and 10.2 μM, respectively .
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Cat. No.: HY-P10304C
CAS No.: 181961-24-0
Target:  

Fungal

Research Areas:  

Infection

Cyclo(Pro-dArg) is an inhibitor of chitinase. Cyclo(Pro-dArg) inhibits the cell separation of Saccharomyces cerevisiae but does not affect its growth. Cyclo(Pro-dArg) inhibits the transition of Candida albicans from yeast to filamentous morphology.
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Cat. No.: HY-P10053
CAS No.: 236394-37-9
Target:  

Phospholipase

Research Areas:  

Metabolic Disease

sPLA2-IIA Inhibitor is a cyclic pentapeptide analog of FLSYK (cyclic 2-Nal-Leu-Ser-2-Nal-Arg (c2)), that binds to hGIIA (human IIA phospholipase A2) and inhibits its hydrolytic ability. sPLA2 is a member of the esterase superfamily that catalyzes the hydrolysis of the ester bond at the sn-2 position of glycerophospholipids, releasing free fatty acids such as arachidonic acid and lysophospholipids .
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Cat. No.: HY-P3472
CAS No.: 57089-60-8
Synonyms: Cyclo(L-Pro-L-Ile)
Research Areas:  

Inflammation/Immunology

Cyclo(IP) (Cyclo-(L-Pro-L-Ile)), a Diketopiperazine can be derived From Bacillus thuringiensis JCK-1233, results in suppression of PWD severity and increased the expression of defense-related genes similarly to Bacillus thuringiensis JCK-1233 treatment .
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Cat. No.: HY-P5050
CAS No.: 227777-31-3
Target:  

Peptides

Research Areas:  

Others

Cyclo(Pro-Thr) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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Cat. No.: HY-P5751
CAS No.: 104068-43-1
Cyclo(Ile-Val) is a Alkaloids product that can be isolated from the roots of Panax notoginseng (Burk.)F.H.Chen .
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Cat. No.: HY-P11224
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

RMI-L4 is an efficient cyclic peptide inhibitor that can specifically disrupt the interaction between FANCM and RMI proteins with an IC50 of 54 nM. RMI-L4 engages the FANCM-binding pocket of RMI1/2 with nanomolar affinity (KD = 2.5 nM). RMI-L4 cannot penetrate the cell membrane and can be used to study the FANCM-RMI pathway targeting cancer with alternate lengthening of telomeres (ALT) .
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Cat. No.: HY-P5036
CAS No.: 852955-00-1
Target:  

Peptides

Research Areas:  

Others

Cyclo(D-Trp-Tyr) is aCyclic dipeptide.
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Cat. No.: HY-W010216S
CAS No.: 1220905-42-9
Synonyms: 4-tert-Butylcyclohexanone-d9
4-(tert-Butyl)cyclohexanone-d9 is the deuterium labeled 4-(tert-Butyl)cyclohexanone .
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Cat. No.: HY-Y0421
CAS No.: 700-58-3
Synonyms: 2-Adamantone; 2-Oxoadamantane
Target:  

11β-HSD

Research Areas:  

Others

Adamantanone (2-Adamantone; 2-Oxoadamantane) serves as a substrate for some alcohol dehydrogenases and also acts as a probe for characterizing substrate-binding pockets. Adamantanone can be reduced by 3α-hydroxysteroid dehydrogenase and 3β-17β-hydroxysteroid dehydrogenase derived from Pseudomonas testosteroni, and it can fit into the conformationally flexible substrate-binding pockets of these enzymes that undergo substrate-induced fit .
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Cat. No.: HY-W699022
CAS No.: 873928-71-3
Synonyms: Tramadol Impurity E-d6 (Y0000157)
2-((Dimethylamino)methyl)cyclohexanone-d6 (Tramadol Impurity E-d6 (Y0000157)) is the deuterium labeled 2-((Dimethylamino)methyl)cyclohexanone (HY-W098651).
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Cat. No.: HY-P1937
CAS No.: 53049-06-2
Target:  

Influenza Virus

Research Areas:  

Infection

Cyclo(-Met-Pro) is a cyclic dipeptide consisting of the amino acids methionine and proline. Cyclo(-Met-Pro) exhibits weak inhibitory activity against the influenza A virus (H3N2) (5 mM, 2.1% inhibition), while cis-cyclo(Leu-Pro) and cis-cyclo(Phe-Pro) shows significant antiviral activity .
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Cat. No.: HY-P5038
CAS No.: 135432-37-0
Synonyms: c(GRGDSP)
Target:  

Integrin

Research Areas:  

Cancer

Cyclo(Gly-Arg-Gly-Asp-Ser-Pro) (c(GRGDSP)) is an RGD-containing inhibitory peptide. Cyclo(Gly-Arg-Gly-Asp-Ser-Pro) is a synthetic α5β1 integrin ligand that competitively inhibits the binding of invasin (Inv) to α5β1 integrin expressed on Caco-2 cells .
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Cat. No.: HY-W836186
CAS No.: 24676-83-3
Synonyms: Cyclo(alanine-leucine)
Target:  

Bacterial

Research Areas:  

Others

Cyclo(Leu-Ala) (Cyclo(alanine-leucine)) is an antimicrobial compound isolated from microorganisms and has antimicrobial activity against some plant pathogens together with other compounds.
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Cat. No.: HY-P10223
Research Areas:  

Cancer

Cyclo CRVIIF is a dual inhibitor for hypoxia inducible factor (HIF) 1 and 2, which disrupts the interaction of both HIF1-α and HIF2-α with HIF1-β, with affinity for HIF1-α and HIF2-α PAS-B domains KD of 65 and 123 μM, respectively .
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Cat. No.: HY-P10812
CAS No.: 1631984-43-4
Target:  

Peptides

Research Areas:  

Cancer

CP61, a cyclic peptide, is a dual CtBP1/CtBP2 inhibitor. CP61 binds CtBP1 with 3 μM affinity. CP61 inhibits the heterodimerization and homodimerization of CtBP2 with an IC50 value of 19 μM. CP61 is promising for research of cancers .
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